DTS Regulatory

Your Goals, Our Expertise
Achieve Your Product Registration And Approvals With Us

Take Advantage Of Our Experience And Knowledge

DTS Regulatory Consulting is a group of specialised scientists. We work with our clients to provide solutions to their regulatory requirements in Australia and New Zealand.
Our consultants are experienced in successfully working with the Regulatory Authorities to achieve registration for a wide range of products including agriculture, complimentary medicines, veterinarian, medical devices, industrial chemicals and cosmetics.

The strength of DTS lies in our collaborative approach to problem solving, internally and externally. Project leadership and peer reviews are shared amongst all consultants. The outcome of this collaborative approach is the depth of knowledge that we can offer our clients.

Over the past 30 years DTS has submitted over 1500 applications to the various regulatory bodies in Australia and New Zealand. Each one of those applications have provided new information that has been added to our knowledge bank.

If negotiating the regulatory environment is important to your organisation’s future then let us join your team and be part of a successful collaborative approach.

Years Experience

Submitted Applications

News

Disinfectants with Antiviral Claims

Disinfectants with Antiviral Claims

Due to the COVID-19 pandemic, there has been significant interest from potential sponsors and manufacturers in producing and selling disinfectants and other related products to the Australian market. There is specific interest on whether claims made to remove, kill,...

The Tale Of Restricting Agrochemicals – Sri Lanka

The Tale Of Restricting Agrochemicals – Sri Lanka

In May 2021 the Sri Lankan government banned the importation of fertilizers and agrochemicals including insecticides and herbicides. The new regulation lead to widespread concern among Sri Lanka’s farming community, industry associations, practitioners, and...

Long Awaited Update for Medical Devices

Long Awaited Update for Medical Devices

The TGA published an updated version of the Essential Principles Checklist applicable to medical devices and In-vitro diagnostic devices (IVDs). The change involved the addition of requirements in relation to programmed or programmable medical devices or...